CTRI/2024/07/069697尚未招募不适用
A prospective randomized, comparative study of Dexmedetomidine Vs Dexamethasone as an adjuvant to Ropivacaine in Usg Guided Erector Spinae Plane Block for Patients Undergoing Laproscopic Cholecystectomy
Dr Uppala Eswar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年9月7日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- To study the duration of postoperative analgesia
研究概览
简要总结
This trial is to compare the effect of Inj Ropivacaine along with Inj. Dexmed and Inj Dexamethasone as an adjuvant in Erector spinae muscle block post lap cholecystectomy . We will be studying the efficacy and duration of the block in this study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •ASA grade I and grade II Patients
- •Age- 20 to 60 years of either sex
- •Weight of patient ranging 50-70 kg.
- •Patients undergoing elective laparoscopic cholecystectomy.
排除标准
- •Patient refusal to ESPB,
- •â‰¥ Patients with ASA physical status III-IV,
- •Infection at injection site,
- •Coagulopathy or bleeding disorder, bradycardia, cardiac conduction block, were administered B-adrenergic antagonist or an antiplatelet agent, s Any systemic illness like DM, HTN etc
- •1st 2nd and 3rd deggree heart block
- •Known allergy or hypersensitivity to local anaesthetic drugs.
结局指标
主要结局
To study the duration of postoperative analgesia
时间窗: Injection will be given and Post operative pain assessment will be assessed at 5 mins, 10 mins, 15 mins, 20 mins, 25 mins, 30 mins, 60 min, 120 min, 240 mins, 360 mins and 12th hour and 24th hour
次要结局
- Total rescue analgesia consumption in 24 hrs.(2. Duration of sensory block)
研究者
研究点 (1)
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